Chunfeng Hu

Prof. Dr. Chunfeng Hu

School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan, China
orcid
Full professor

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 August 2018 in Ceramics International
Verified
Journal Article
Closed access
LXLudi Xu
Ludi Xu
OSOuling Shi
Ouling Shi
CLCaiyun Liu
Caiyun Liu
DZDegui Zhu
Degui Zhu
SGSalvatore Grasso
Salvatore Grasso
Chunfeng HuChunfeng Hu
Chunfeng Hu

1 October 2021 in Journal of the European Ceramic Society
Verified
Journal Article
Closed access
MKMilad Kermani
Milad Kermani
JDJian Dong
Jian Dong
Mattia BiesuzMattia Biesuz
Mattia Biesuz
YLYong Linx
Yong Linx
HDHuaijiu Deng
Huaijiu Deng
Salvatore GrassoSalvatore Grasso
Salvatore Grasso

30 March 2019 in Journal of Asian Ceramic Societies
Verified
Journal Article
Open access
Mattia BiesuzMattia Biesuz
Mattia Biesuz
SFShuai Fu
Shuai Fu
JDJian Dong
Jian Dong
AJAnna Jiang
Anna Jiang
DKDaoyao Ke
Daoyao Ke
SGSalvatore Grasso
Salvatore Grasso
A rising interest in entropy-stabilized oxides in recent years has been driven by their attractive functional properties. Their synthesis usually requires prolonged exposure at high temperature to promote solid-state diffusion without the application of pressure. In this work, we report the synthesis of a high entropy perovskite, Sr((Zr0.94Y0.06)0.2Sn0.2Ti0.2Hf0.2Mn0.2)O3−x, in a relatively short time (minutes instead of hours) using a spark plasma sintering (SPS) furnace. Comparative analysis showed that conventional pressureless sintering at 1500°C for 2 h results in porous materials with large thermodynamically stable pores (tens of µm), while SPS processing produces dense materials in a single step by reactive sintering at 1475°C in 9 min. SPS is therefore an attractive route for the production, synthesis and sintering of dense high-entropy oxides.

27 July 2020 in Journal of Advanced Ceramics
Verified
Journal Article
Open access
PDF file
QXQiang Xu
Qiang Xu
YZYanchun Zhou
Yanchun Zhou
HZHaiming Zhang
Haiming Zhang
AJAnna Jiang
Anna Jiang
QTQuanzheng Tao
Quanzheng Tao
Chunfeng HuChunfeng Hu
Chunfeng Hu
Guided by the theoretical prediction, a new MAX phase V2SnC was synthesized experimentally for the first time by reaction of V, Sn, and C mixtures at 1000 °C. The chemical composition and crystal structure of this new compound were identified by the cross-check combination of first-principles calculations, X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), and high resolution scanning transmission electron microscopy (HR-STEM). The stacking sequence of V2C and Sn layers results in a crystal structure of space group P63/mmc. The a- and c-lattice parameters, which were determined by the Rietveld analysis of powder XRD pattern, are 0.2981(0) nm and 1.3470(6) nm, respectively. The atomic positions are V at 4f (1/3, 2/3, 0.0776(5)), Sn at 2d (2/3, 1/3, 1/4), and C at 2a (0, 0, 0). A new set of XRD data of V2SnC was also obtained. Theoretical calculations suggest that this new compound is stable with negative formation energy and formation enthalpy, satisfied Born-Huang criteria of mechanical stability, and positive phonon branches over the Brillouin zone. It also has low shear deformation resistance c44 (second-order elastic constant, cij) and shear modulus (G), positive Cauchy pressure, and low Pugh’s ratio (G/B = 0.500 < 0.571), which is regarded as a quasi-ductile MAX phase. The mechanism underpinning the quasi-ductility is associated with the presence of a metallic bond.

9 November 2022 in Ceramics International
Verified
Journal Article
Closed access
MKMilad Kermani
Milad Kermani
Chunfeng HuChunfeng Hu
Chunfeng Hu
Salvatore GrassoSalvatore Grasso
Salvatore Grasso

1 February 2019 in Ceramics International
Verified
Journal Article
Closed access
OSOuling Shi
Ouling Shi
LXLudi Xu
Ludi Xu
AJAnna Jiang
Anna Jiang
QXQiang Xu
Qiang Xu
YXYoutao Xiao
Youtao Xiao
Chunfeng HuChunfeng Hu
Chunfeng Hu